Thermoplastic moulding compositions based on polysiloxane/polycarbonate block copolymers

ABSTRACT

The present invention relates to 
     A. Thermoplastic moulding materials based on polydiorganosiloxane/polycarbonate block copolymers and ABS polymers and 
     B. Thermoplastic moulding compositions based on polysiloxane/polycarbonate block copolymers, elastomeric polymers and, if appropriate, polyalkylene terephthalate.

The present invention relates to A. Thermoplastic moulding compositionsbased on polydiorganosiloxane/polycarbonate block copolymers and ABSpolymers and B. Thermoplastic moulding compositions based onpolysiloxane/polycarbonate block copolymers, elastomeric polymers and,if appropriate, polyalkylene terephthalate.

A. Thermoplastic mixtures of polycarbonates based on aromatic dihydroxycompounds and ABS polymers are known in principle (German PatentSpecification No. 1,170,141 and German Auslegeschrift No. 1,810,993).Mixtures of aromatic polycarbonates with special ABS systems aredescribed in German Patent Specification No. 2,259,565 (Le A 14 751),German Offenlegungsschrift No. 2,329,548 (Le A 15 106) and GermanOffenlegungsschrift No. 2,329,546 (Le A 15 107).

Such mixtures have to meet very high technological requirements. In thiscontext, in particular, good toughness, especially at low temperatures,and improvements in the fire behaviour (tendency to drip) are required.

To date, these types of improvements in the properties could be achievedonly by selective variation of the rubber and the additional use offlameproofing agents.

It was therefore surprising that this improved overall spectrum ofproperties could be achieved merely by the use of a modifiedpolycarbonate. It was also surprising that when the polycarbonatemodified with a diorganosiloxane block was mixed with ABS polymers,moulding compositions having good properties were obtained, in sprite ofthe Si block.

Although European Offenlegungsschrift No. 0,073,067 discloses mixturesof aromatic polyesters, siloxane/polycarbonate block copolymers andthermoplastic styrene resins or thermoplastic alkyl acrylate resins, noparticular technical advantages are claimed for the addition of styreneresin or alkyl acrylate resin.

The present invention relates to thermoplastic moulding compositionsbased on aromatic polycarbonates and ABS polymers, which have improvedtoughness when subjected to impact (notched impact strength), inparticular at low temperatures, as well as better fire behaviour,characterised by a higher oxyen index and improved drippingcharacteristics.

The present invention thus relates to thermoplastic mouldingcompositions containing (a) 20-80 parts by weight of apolydiorganosiloxane polycarbonate block copolymer which has a meanmolecular weight M_(w) of 10,000 to 200,000 and contains between about75% by weight and 97.5% by weight of aromatic carbonate structural unitsand contains between 25% by weight and 2.5% by weight ofpolydiorganosiloxane structural units, the block copolymers beingprepared from polydiorganosiloxanes which contain αω-bishydroxyaryloxyterminal groups and have a degree of polymerisation P_(n) of 5-100,

(b) 70-5 parts by weight of a graft polymer of ethylenically unsaturatedmonomers on rubbers from the series comprising diene monomer, alkylacrylate and EPDM rubbers, and

(c) 5-60 parts by weight of a rubber-free thermoplastic polymer of vinylmonomers, the sum of the number of parts by weight of components(a)+(b)+(c) being 100 parts by weight in each case.

The component (a) can also be a mixture ofpolydiorganosiloxane/polycarbonate block copolymers with customarypolysiloxane-free thermoplastic polycarbonates, the total content ofpolydiorganosiloxane structural units in this mixture being between 2.5and 25% by weight.

In the context of the invention, polydiorganosiloxane/polycarbonateblock copolymers (a) are reaction products obtained from diphenol, theirreactive derivatives based on polydiorganosiloxane oligomers withreactive terminal groups or mixtures of the oligomers, carbonic acidprecursors or mixtures of these reaction products.

Such polydiorganosiloxane/polycarbonate block copolymers arecharacterised in that they contain, in the polymer chain, aromaticcarbonate structural units (1) on the one hand, andpolydiorganosiloxanes containing aryloxy terminal groups (2) on theother hand ##STR1## wherein Ar are identical or different aryleneradicals obtained from diphenols, and

R and R¹ are identical or different and denote linear alkyl, branchedalkyl, alkenyl, halogenated linear alkyl, halogenated branched alkyl,aryl or halogenated aryl, but preferably methyl, and

the number of diorganosiloxy units n (=a+b+c) is 5 to 100, preferably 20to 80.

In the above formula (1), alkyl is, for example, C₁ -C₂₀ -alkyl; in theabove formula (1), alkenyl is, for example, C₂ -C₆ -alkenyl; in theabove formula (1), aryl is C₆ -C₁₄ -aryl. In the above formula,halogenated denotes partially or completely chlorinated, brominated orfluorinated. Examples of alkyls, alkenyls, aryls, halogenated alkyls andhalogenated aryls are methyl, ethyl, propyl, n-butyl, tert.-butyl,vinyl, phenyl, naphthyl, chloromethyl, perfluorobutyl, perfluorooctyland chlorophenyl.

Polydiorganosiloxane/polycarbonate block copolymers of this type aredisclosed in, for example, U.S. Pat. Nos. 3,189,662, 3,821,325 and3,832,419. Their improved mechanical properties at low temperatures aredescribed in the relevant literature (for example B. M. Beach, R. P.Kambour and A. R. Schultz, J. Polym. Sci., Polym. Lett. Ed. 12, 247(1974)).

Preferred polydiorganosiloxane/polycarbonate block copolymers havingmean molecular weights M_(w) (weight average, as determined byultracentrifuging or a light scattering measurement) of 10,000 to200,000 and containing between about 75% by weight and 97.5% by weightof aromatic carbonate structural units and containing between 25 and2.5% by weight of diorganosiloxy units are prepared by reactingpolydiorganosiloxanes containing α,β-bishydroxyaryloxy terminal groupswith other diphenols, if appropriate with the concomitant use of chainterminators in the customary amounts, and if appropriate with theconcomitant use of branching agents in the customary amounts, forexample by the two-phase boundary method (in this context, see H.Schnell, Chemistry and Physics of Polycarbonates, Polymer Rev., Vol. IX,page 27 et seq., Interscience Publishers New York, 1964), the ratio ofthe bifunctional phenolic reactants is chosen in each case so that itgives the content, according to the invention, of aromatic carbonatestructural units and diorganosiloxy units.

Such polydiorganosiloxanes containing α,β-bishydroxyaryloxy terminalgroups are disclosed in, for example, U.S. Pat. No. 3,419,634.

Diphenols to be employed for the preparation of thepolydiorganosiloxanes containing α,ω-bishydroxyaryloxy terminal groupsand of the polydiorganosiloxane/polycarbonate block copolymers arehydroquinone, resorcinol, dihydroxydiphenyls,bis-(hydroxyphenyl)-alkanes, bis-(hydroxyphenyl)-cycloalkanes,bis-(hydroxyphenyl) sulphides, bis (hydroxyphenyl) ethers,bis-(hydroxyphenyl) sulphoxides, bis-(hydroxyphenyl) sulphones andα,ω-bis(hydroxyphenyl)-diisooropylbenzenes and their compounds which arealkylated in the nucleus and halogenated in the nucleus. These and othersuitable aromatic dihydroxy compounds are listed in the U.S. Pat. Nos.3,028,365 and 2,999,846 and in the German Offenlegungsschriften Nos.2,063,050 and 2,211,957.

Examples of preferred diphenols are 2,2-bis-(4-hydroxyphenyl)-propane,1,1-bis-(4-hydroxyphenyl)-cyclohexane,2,2-bis-(3,5-dichloro-4-hydroxyphenyl)-propane,2,2-bis-(3,5-dibromo-4-hydroxyphenyl)-propane,2,2-bis(3,5-dimethyl-4-hydroxyphenyl)-propane,bis-(3,5-dimethyl4-hydroxyohenyl)-methane and bis-(4-hydroxyphenyl)sulphide.

The suitable diphenols can be employed both alone and as mixtures.

Branching agents which can be used are those having three or more thanthree functional groups, in particular those having three or more thanthree phenolic hydroxyl groups, and the customary known amounts ofbranching agent of between 0.05 and 2 mol %, relative to diphenolsincorporated, should be maintained. The preparation of branchedpolycarbonates is described in, for example, German OffenlegungsschriftNos. 1,570,533 and 1,595,762 and in U.S. Pat. No. 3,544,514.

Examples of some of the usable compounds having three or more than threephenolic hydroxyl groups are 2,4-bis-(4-hydroxyohenyl-isopropyl)-phenol,2,6-bis-(2'-hydroxy-5'-methyl-benzyl)-4-methylphenol,2-(4-hydroxyphenyl)-2-(2,4-dihydroxyphenyl)-propane and1,4-bis-(4,4'-dihydroxytriphenyl-methyl)-benzene. Some of the othertrifunctional compounds are 2,4-dihydroxybenzoic acid, trimesic acid,cyanuric chloride and 3,3-bis-(4 -hydroxyphenyl)-2-oxo-2,3-dihydroindoleas well as 3,3-bis-(4-hydroxy-3-methyl-phenyl)-2-oxo-2,3-dihydroindole.

Compounds which can be used as chain terminators in the preparation bythe two-phase boundary method are aromatic compounds containing afunctional group, such as aromatic acid halides or phenols, inparticular the conventional phenols, such as, for example,p-tert.-butylphenol, p-chlorophenol, 2,4,6-tribromophenol and phenol,these being used in the customary amount, which is governed by themolecular weight to be achieved in each case for the block copolymersaccording to the invention. In general, 0.5 mol % to 10.0 mol %,relative to diphenols employed, are used.

In the context of the invention, graft polymers (b) are those in whicheither a monomer from the styrene series, methyl methacrylate or amonomer mixture of 95-50% by weight of styrene,α-methylstyrene, methylmethacrylate or mixtures thereof and 5-50% by weight of acrylonitrile,methyl methacrylate, maleic anhydride, N-substituted maleimides ormixtures thereof are grafted on to a rubber. Suitable rubbers are, inparticular, polybutadiene, butadiene/styrene copolymers containing up to30% by weight of styrene as copolymerised units, copolymers of butadieneand acrylonitrile containing up to 20% by weight of acrylonitrile, orcopolymers of butadiene containing up to 20% by weight of a lower alkylester of acrylic or methacrylic acid (for example methyl acrylate, ethylacrylate, methyl methacrylate and ethyl methacrylate).

Examples of other suitable rubbers are polyisoprene or polychloroprene.Alkyl acrylate rubbers based on C₁ -C₈ -alkyl acrylates, in particularethyl, butyl or ethylhexyl acrylate, are also suitable. These alkylacrylate rubbers can, if appropriate, contain up to 30% by weight ofmonomers, such as vinyl acetate, acrylonitrile, styrene, methylmethacrylate or vinyl ether, as copolymerised units. These alkylacrylate rubbers can furthermore contain relatively small amounts (up to50% by weight) of crosslinking ethylenically unsaturated monomers.Examples of such comoounds are alkylenediol di(meth) acrylates,polyester di(meth) acrylates, di- and tri-vinylbenzene, triallylcyanurate, allyl (meth) acrylate, butadiene, isoprene etc. Such alkylacrylates are known. Acrylate rubbers used as a grafting base can alsobe products which contain, as a core, a crosslinked diene rubberconsisting of one or more conjugated dienes, such as polybutadiene, or acopolymer of a conjugated diene with an ethylenically unsaturatedmonomer, such as styrene and/or acrylonitrile. Examples of othersuitable rubbers are EPDM rubbers, that is to say rubbers obtained fromethylene, prooylene and an unconjugated diene monomer.

Diene monomer rubbers or alkyl acrylate rubbers are preferred.

The graft copolymers (b) contain 5-80% by weight, in particular 20-70%by weight, of rubber and 95-20% by weight, in particular 80 to 30% byweight, of grafted monomers. The rubbers are present in these graftcopolymers in the form of at least partially crosslinked particleshaving a mean particle size from 0.09 to 5 μm, in particular from 0.1 to1 μm. Graft copolymers of this type are prepared by free-radical graftcopolymerisation of monomers from the series comprising styrene,α-methylstyrene, acrylonitrile, methyl methacrylate and maleic anhydridein the presence of the rubbers to be grafted, and are all known.Preferred preparation processes for such graft copolymers are emulsionpolymerisation, solution polymerisation, mass polymerisation orsuspension polymerisation.

So-called ABS polymers are particularly preferred.

The rubber-free polymers of vinyl monomers (c) can be composed of thegraft monomers or similar monomers, in particular of at least onemonomer from the series comprising styrene,α-methylstyrene,halogenostyrene, acrylonitrile, methacrylonitrile, methyl methacrylate,maleic anhydride, vinyl acetate and N-substituted maleimide. They arepreferably copolymers consisting of 95-50% by weight ofstyrene,α-methylstyrene, methyl methacrylate or mixtures thereof, with5-50% by weight of acrylonitrile, methacrylonitrile, methylmethacrylate, maleic anhyride or mixtures thereof. Such copolymers arefrequently formed in graft copolymerisation as by-products, particularlywhen large amounts of monomers are grafted onto small amounts of rubber.In addition to, or instead of, the copolymers thus formed, it is alsopossible to admix separately prepared copolymers of this type. On theother hand, the ungrafted resin moieties present in the graft polymersneed not necessarily be chemically identical to the admixedthermoplastic vinyl polymer (c).

Separately prepared copolymers of this type are resin-like,thermoplastic and rubber-free; they are, in particular, copolymers ofstyrene and/or α-methylstyrene with acrylonitrile, if appropriate mixedwith methyl methacrylate.

Particularly preferred copolymers consist of 20-40% by weight ofacrylonitrile and 80-60% by weight of styrene or α-methylstyrene. Suchcopolymer materials are known, and can be prepared, in particular, byfree-radical polymerisation processes, in particular by emulsionpolymerisation, suspension polymerisation, solution polymerisation ormass polymerisation. The copolymers preferably have molecular weights of15,000 to 2·10⁵.

The moulding compositions according to the invention can be obtained bymixing the individual components. In a preferred preparation method, alatex of a graft copolymer (b) is first precipitated and dried. Thepowder thus obtained is then mixed with the polydiorganosiloxanepolycarbonate block copolymer (a) and the separately prepared copolymer(c).

For example, roll mills, screw extruders or kneaders are suitable forthis purpose.

Either the individual components of the moulding compositions accordingto the invention contain additives, such as stabilisers, oigments,free-flow aents, lubricants, mould-release agents, antistatics and/orflameproofing agents, or these additives can be added during mixing ofthe individual components. Suitable additives are those which arecustomary for thermoplastic polycarbonates, graft polymers orthermoplastic vinyl polymers.

The moulding compositions of the present invention can be used for theproduction of shaped articles of any kind. In particular, shapedarticles can be produced by injection moulding. Examples of shapedarticles which can be produced are: housing components of any kind (forexample for household appliances, such as juice extractors, coffeemachines and mixers) or cover plates for the building sector andcomponents for the automobile sector. They are also employed in thefield of electrotechnology, because they are distinguished by very goodelectrical properties.

In the examples which follow, the followingpolydiorganosiloxane/polycarbonate block copolymers were used:

(a1) A copolycarbonate based on bisphenol A and 4.5% by weight ofpolydimethylsiloxane having a block length (P_(n)) of 40, with arelative solution viscosity of 1.31, measured in CH₂ Cl₂ at 25° C. and aconcentration of 0.5% by weight.

(a2) A copolycarbonate based on bisphenol A and 10% by weight ofpolydimethylsiloxane having a block length (P_(n)) of 40, with arelative solution viscosity of 1.29.

(a3) A comparative polycarbonate based on bisphenol A, with a relativesolution viscosity of 1.29.

(a4) A copolycarbonate according to (a1), except that it contains 5% byweight of polydimethylsiloxane and has a relative solution viscosity of1.29.

The determination of the siloxane content, that is to say the proportionof dimethylsiloxy units in % by weight, relative to the total weight ofthe block copolymer, is carried out gravimetrically and by means ofnuclear resonance spectrometry. The mean siloxane block length is statedas the degree of polymerisation P_(n) found by determining the terminalgroups in the siloxane prepolymer.

For the examples listed, the components (b) and (c) were used as an ABSpolymer.

(b) 40 parts by weight of a graft polymer, prepared by grafting 35 partsby weight of styrene and 15 parts by weight of acrylonitrile onto 50parts by weight of a coarse-particled polybutadiene (obtained viaemulsion polymerisation, according to the preparation data of GermanAuslegeschriften Nos. 1,247,665 and 1,269,360), the mean particlediameter of the polybutadiene grafting base present in latex form beingbetween 0.3 and 0.4 μm. (This particle size information and thecorresponding information in the text represent mean particle diameters(d₅₀) and are determined by ultracentrifuge measurement (in thiscontext, see: W. Scholtan et al. Colloids. Z. Polymere, 250 (1972),pages 783-796);

(c) 60 parts by weight of a styrene/acrylonitrile copolymer having astyrene/acrylonitrile ratio of 70:30 and an intrinsic viscosity of[η]=0.79 dl/g (measured in dimethylformamide at 20° C.)

The moulding compositions of the examples below were prepared in atwin-screw extruder at about 260° C., by mixing the individualcomponents.

The notched impact strength and the impact strength were determined onstandard small bars, on the basis of DIN No. 53,453/ISO R 179. The Vicatheat-distortion resistance was determined in accordance with DIN No.53,460. The oxygen index was determined on 10 standard small bars, inaccordance with ASTM-D 2863. The dripping behaviour was determined usingbars having the dimensions 127×12.7× 3.2 mm. For this purpose, groups of5 specimens were ignited by means of two successive ignition processesof 10 seconds duration, and the number of specimens dripping flamingparticles was determined. The experimental arrangement corresponded tothe data stated according to UL 94 (Underwriters' Laboratories, Inc.)for the UL 94 V test.

    ______________________________________                                        Examples                                                                                  Dimen-                                                                              (compar.)                                                   Composition   sion    1.      2.    3.     4.                                 ______________________________________                                        Copolycarbonate a1                                                                          %       70      --    --    --                                  Copolycarbonate a2                                                                          %       --      70    --    --                                  Homopolycarbonate a3                                                                        %       --      --    70    --                                  Copolycarbonate a4                                                                          %       --      --    --    70                                  Polymer b + c %       30      30    30    30                                  Notched impact strength                                                       at room temperature                                                                         kJ/m.sup.2                                                                             43*    29    23    25                                  at -20° C.                                                                           kJ/m.sup.2                                                                             47*    --    12    19                                  at -40° C.                                                                           kJ/m.sup.2                                                                            29      23     9    20                                  Vicat B temperature                                                                         °C.                                                                            131     122   127   127                                 O.sub.2 index %         26.0    25.5                                                                                23.5                                                                              --                                  Number of specimens    0       0     5     0                                  dripping flaming                                                              particles                                                                     ______________________________________                                         *fractured                                                               

B.

Mixtures of polycarbonates and polymers are known (see, for example,Japanese Patent Publication No. 18 611 68 (Teijin, Priority 30.6.65),U.S. Pat. Nos. 3,663,471 (Le A 11 969), 3,437,631 (Mo 936), 4,299,928(Mo 2062) or German Offenlegungsschrift No. 3,114,494).

Compared with pure polycarbonate, such mixtures have improved toughnessproperties.

Thermoplastic moulding compositions based onpolydiorganosiloxane/polycarbonate block copolymers and polyalkyleneterephthalates are known; see, for example, U.S. Pat. Nos. 4,161,469 and4,161,498. They are said to be distinguished by improved impact strengthand heat-distortion resistance.

European Offenlegungsschrift No. 0,073,067 discloses mixtures ofaromatic polyesters, siloxane/polycarbonate block copolymers, polyestersof diols with aromatic dicarboxylic acids and thermoplastic styreneresins or thermoplastic alkyl acrylate resins, which are distinguishedby improved notched impact strength compared with the aromaticpolyesters.

Although the stated moulding compositions possess many advantageousproperties, they do not meet some special requirements, as set, forexample, for device components in the engine space of motor vehicles,such as heat-distortion resistance, freedom from distortion, resistanceto petrol and good toughness at low temperatures.

Surprisingly, it has now been found that mixtures of apolydiorganosiloxane/polycarbonate block copolymer and an elastomericpolymer having a glass transition temperature below -20° C. exhibit highheat-distortion resistance as well as a transition, between the toughstate and the brittle-state, which is substantially shifted toward lowertemperatures.

If it is necessary to have particularly high resistance to petrolcoupled with an otherwise constant spectrum of properties, it isappropriate to add polyalkylene terephthalate.

The invention relates to thermoplastic moulding compositions containing:

(a) 10-98, preferably 30-90, parts by weight of apolydiorganosiloxane/polycarbonate block copolymer having a meanmolecular weight M_(w) of 10,000 to 200,000 and containing between 75%by weight and 97.5% by weight of aromatic carbonate structural units andcontaining between 25% by weight and 2.5% by weight ofpolydiorganosiloxane structural units, the block copolymers beingprepared from polydiorganosiloxanes which contain α,ω-bis-hydroxyaryloxyterminal groups and have a degree of polymerisation P_(n) of 5 to 100,

(d) 1-30, preferably 5-20, parts by weight of elastomeric polymershaving a glass transition temperature of below -20° C. and

(e) 0-50 parts by weight of thermoplastic polyalkylene tereohthalates,the sum of the number of parts by weight of components (a)+(d)+(e) being100 parts by weight in each case.

The component (a) can also be a mixture ofpolydiorganosiloxane/polycarbonate block copolymers containing customarypolysiloxane-free thermoplastic polycarbonates, the total content ofpolydiorganosiloxane structural units in this mixture being between 2.5and 25% by weight.

The polydiorganosiloxane/polycarbonate block copolymers are the blockcopolymers characterised in Part A.

The elastomeric polymers (d) comprise copolymers, in particular graftcopolymers, which have elastomeric properties and are essentiallyobtainable from at least two of the following monomers: chloroprene,butadiene, isoprene, isobutene, styrene, acrylonitrile, ethylene,propylene, vinyl acetate, (meth) acrylates having 1-18 C atoms in thealcohol component, and carbon monoxide, that is to say polymers asdescribed in, for example, "Methoden der Organischen Chemie" ("Methodsof Organic Chemistry"), (Houben-Weyl), Vol. 14/1, Georg Thieme-Verlag,Stuttgart 1961, pages 393-406, and in C. B. Bucknall, "ToughenedPlastics", Appl. Science Publishers, London 1977. Preferred polymers forcomponent (d) have a gel content of more than 20, preferably more than40%, by weight.

Preferred polymers for component (d) are ethylene vinyl acetatecopolymers containing 15-70% by weight of vinyl acetate and having meltindices from non-free-flowing to 1,000, preferably 0.1-20, measured at190° C. and with a load of 2.16 kp, in accordance with DIN 53,753.Terpolymers obtained from ethylene, alkyl acrylates or vinyl acetate andcarbon monoxide are also preferred.

Examples of preferred polymers for component (d) are the so-called EPMand EPDM rubbers, in which the weight ratio of ethylene radicals topropylene radicals is in the range from 40:60 to 90:10, preferably 40:60to 65:35.

The Mooney viscosities (ML 1+4/100° C. in accordance with DIN 53,523) ofthe non-crosslinked EPM and EPDM rubbers are between 25 and 100 MU,preferably between 35 and 90 MU. The gel contents of the non-crosslinkedEPM and EPDM rubbers are below 1% by weight.

The ethylene/propylene copolymers (EPM) used contain virtually no doublebonds, whereas the ethylene propylene/diene terpolymers (EPDM) cancontain 1-20 double bonds/1,000 C atoms. Examples of suitable dienemonomers in EPDM which may be mentioned are conjugated dienes, forexample isoprene and butadiene, and nonconjugated dienes having 5-25 Catoms, for example 1,4-pentadiene, 1,4-hexadiene, 1,5-hexadiene,2,5-dimethyl-1,5-hexadiene and 1,4-octadiene, cyclic dienes, for examplecyclopentadiene, cyclohexadiene, cyclooctadiene and dicyclopentadiene;alkenylnorbornenes, for example 5-ethylidene-2-norbornene,5-butylidene-2-norbornene, 2-methallyl-5-norbornene and2-isopropenyl-5-norbornene, and tricyclodienes, for example3-methyltricyclo-(5,2,1,0,2,6)3,8-decadiene. The non-conjugated dienes1,5-hexadiene, ethylidenenorbornene and dicyclopentadiene may bepreferably mentioned. The diene content in the EPDM is preferably 0.5 to10% by weight.

EPM and EPDM rubbers of this type are described in, for example, GermanOffenlegungsschrift No. 2,808,709 (le A 18 705).

Preferred polymers for component (d) are also block copolymers, whichmay be selectively hydrogenated, of a vinyl-aromatic monomer X and aconjugated diene Y, of the X-Y type or X-(Y-X)_(r) type (with r=1-5) orY-(X)_(s) type (with s=3-5).

These block copolymers can be prepared by known processes. In general,the preparation of suitable X-Y block copolymers fromstyrene,α-methylstyrene, vinyl-toluene etc. and from conjugated dienes,such as butadiene, isoprene etc., can be carried out using thetechnology employed for the preparation of styrene/diene blockcopolymers, this technology being described in "Encyclopedia of PolymerScience and Technology", Vol. 15, Interscience, N.Y. (1971), on pages508 et seq. The selective hydrogenation can be carried out in ways whichare in themselves known, and means that the ethylenic double bonds areessentially completely hydrogenated, the aromatic double bondsessentially remaining unaffected. Selectively hydrogenated blockcopolymers of this type are described in, for example, GermanOffenlegungsschrift No. 3,000,282.

Examples of preferred polymers for component (d) are butadiene/styrenecopolymers, poly(meth) acrylates and polybutadienes onto which styreneand/or acrylonitrile and/or (meth)acrylates are grafted, for examplecopolymers of styrene or alkylstyrene and conjugated dienes (high-impactpolystyrene), that is to say copolymers of the type described in GermanOffenlegungsschrift No. 1,694,173 (=U.S. Pat. No. 3,564,077), andbutadiene/styrene or butadiene/acrylonitrile copolymers, polyisobutenes,polyisoprenes or polybutadienes onto which acrylates or methacrylates,vinyl acetate, acrylonitrile, styrene and/or alkylstyrenes are grafted,as described in, for example, German Offenlegungsschrift No. 2,348,377(=U.S. Pat. No. 3,919,353).

Examples of particularly preferred polymers for component (d) are graftpolymers which are obtainable by grafting

I. 10-40, preferably 10-35, in particular 15-25, % by weight, relativeto the grafted product, of at least one (meth)acrylate and/or a mixtureof 10-35, preferably 20-35, % by weight, relative to the mixture, ofacrylonitrile and 65-90, preferably 65-80, % by weight, relative to themixture, of styrene onto

II. 60-90, preferably 65-90, in particular 75-85, % by weight, relativeto the grafted product, of a butadiene polymer containing at least 70%by weight, relative to II, of butadiene radicals as the grafting base,

preferably the proportion of gel in the grafting base II being 70%(measured in toluene), the degree of grafting g being 0.15 to 0.55 andthe mean particle diameter d₅₀ of the graft polymer being 0.2-0.6,preferably 0.3-0.5, μm.

(Meth)acrylates I are esters of acrylic acid or methacrylic acid andmonohydric alcohols having 1-18 C atoms.

The grafting base II can contain, in addition to butadiene radicals, upto 30% by weight, relative to II, of radicals of other ethylenicallyunsaturated monomers, such as, for example, styrene, acrylonitrile, andesters of acrylic or methacrylic acid having 1-4 C atoms in the alcoholcomponent (such as methyl acrylate, ethyl acrylate, methyl methacrylateand ethyl methacrylate). The preferred grafting base II consists of purepolybutadiene.

Since, in the grafting reaction, the graft monomers I are usually notcompletely grafted onto the grafting base II, in accordance with theinvention graft polymers are also understood as meaning those productswhich, in addition to the actual graft polymers, also containhomopolymers and copolymers of the graft monomers I employed. In thecontext of the invention, graft polymers are those which are obtained bygraft polymerisation of vinyl monomers in the presence of a polymer II.

The mean particle size d₅₀ is that diameter above and below which liethe diameters of 50% by weight of the particles in each case. It can bedetermined by means of ultracentrifuge measurements (W. Scholtan and H.Lange, Kolloid. Z. und Z. Polymere 250 (1972), 782-796), or by means ofelectron microscopy followed by particle counting (G. Kampf and H.Schuster, Angew. Makromolekulare Chemie 14, (1970), 111-129), or bymeans of light-scattering measurements.

Other examples of particularly preferred polymers for component (d) aregraft polymers consisting of

III. as the grafting base, 25-98% by weight, relative to component (d),of an acrylate rubber having a

glass transition temperature of below -20° C., and

IV. as the grafting monomers, 2-75% by weight, relative to component(d), of at least one polymerisable ethylenically unsaturated monomerwhose homopolymers or copolymers formed in the presence of III have aglass transition temperature of above 25° C.

The acrylate rubbers III of the polymers for component (d) arepreferably polymers obtained from alkyl acrylates, if appropriate withup to 40% by weight of other polymerisable ethylenically unsaturatedmonomers. If the acrylate rubbers employed as the grafting base III (asdescribed below) are in turn already grafted products having a dienerubber core, the diene rubber core is not taken into account whencalculating the percentages. The preferred polymerisable acrylatesinclude C₁ -C₈ -alkyl esters, for example the methyl, ethyl, butyl,octyl and 2-ethylhexyl esters, halogenoalkyl esters, preferablyhalogeno-C₁ -C₈ -alkyl esters, such as chloroethyl acrylate, andaromatic esters, such as benzyl acrylate and phenethyl acrylate. Theycan be employed alone or as a mixture.

The acrylate rubbers III can be non-crosslinked or crosslinked, but arepreferably partially crosslinked.

In order to achieve crosslinking, it is possible to copolymerisemonomers having more than one polymerisable double bond. Preferredexamples of monomers which effect crosslinking are esters of unsaturatedmonocarboxylic acids having three to eight C atoms and unsaturatedmonohydric alcohols having 3-12 C atoms or saturated polyols having 2-4OH groups and 2-20 C atoms, such as, for example, ethylene glycoldimethacrylate and allyl methacrylate; polyunsaturated heterocycliccompounds, such as, for example, trivinyl and triallyl cyanurate andisocyanurate and tris-acryloyl-s-triazines, in particular triallylcyanurate; polyfunctional vinyl compounds, such as di- andtrivinylbenzene, as well as triallyl phosphate and diallyl phthalate.

Preferred monomers which effect crosslinking are allyl methacrylate,ethylene glycol dimethacrylate, diallyl phthalate and heterocycliccompounds which have at least three ethylenically unsaturated groups.

Particularly preferred monomers which effect crosslinking are the cyclicmonomers triallyl cyanurate, triallyl isocyanurate, trivinyl cyanurate,triacryloylhexahydro-s-triazine and triallylbenzenes.

The amount of monomers which effect crosslinking is preferably 0.02 to5, in particular 0.05-2, % by weight, relative to the grafting base III.

In the case of cyclic monomers which effect crosslinking and have atleast 3 ethylenically unsaturated groups, it is advantageous to restrictthe amount to 1% by weight of the grafting base III.

Examples of preferred "other" polymerisable ethylenically unsaturatedmonomers which, if appropriate, can be used, in addition to theacrylates, for the preparation of the grafting base III areacrylonitrile, styrene, α-methylstyrene, acrylamides, vinyl C₁ -C₆-alkyl ethers, butadiene and isoprene. Acrylate rubbers which arepreferred as the grafting base III are emulsion polymers which have agel content of 60% by weight.

The gel content of the grafting base III is determined at 25° C. indimethylformamide (M. Hoffmann, H. Kromer and R. Kuhn, Polymeranalytik Iand lI, Georg Thieme-Verlag Stuttgart 1977).

Acrylate rubbers used as the grafting base III can also be productswhich contain, as the core, a crosslinked diene rubber consisting of oneor more conjugated dienes, such as polybutadiene, or a copolymer of aconjugated diene with an ethylenically unsaturated monomer, such asstyrene and/or acrylonitrile.

The proportion of the polydirne core in the grafting base III can be 0.1to 80, preferably 10-50, % by weight, relative to III. The shell and thecore, independently of one another, can be non-crosslinked, partiallycrosslinked or highly crosslinked.

Particularly preferred grafting bases III for graft polymers, accordingto component (d), which are based on polyacrylates may have thefollowing composition:

1. Acrylate polymers and copolymers without a diene rubber core and

2. Acrylate polymers and copolymers, which contain a diene rubber core.

The grafting yield, that is to say the quotient of the amount of monomerIV grafted on and the amount of graft monomer IV employed, is as a rule20-80% by weight. The determination can be carried out as described inM. Hoffmann, H. Kromer" and R. Kuhn, Polymeranalytik, Vol. 1, GeorgThieme-Verlag, Stuttgart 1977.

Preferred graft monomers IV are α-methylstyrene, styrene, acrylonitrile,methyl methacrylate or mixtures of these monomers. Preferred graftmonomer mixtures are those of styrene and acrylonitrile in the weightratio 90:10 to 50:50.

Such graft polymers for component (d), based on polyacrylates, aredescribed, for example, in German Auslegeschrift No. 2,444,584 (=U.S.Pat. No. 4,022,748) and in German Offenlegungsschrift No. 2,726,256(=U.S. Pat. No. 4,096,202).

Particularly advantageous graft polymers of this type are obtained if2-20, preferably 2-15, % by weight, relative to (d), of monomer IV aregrafted onto 80-98, preferably 85-97, % by weight, relative to (d), ofthe latex of III, which has been completely broken and suspended inwater, in the absence of suspending agents. The pulverulent graftpolymer obtained can then be dried, and homogenised, in the desiredratio and under the action of shear forces, with the other components,so that the mean particle size d₅₀ of component (d) in the mixtureaccording to the invention is 0.05-3, preferably 0.1-2, in particular0.2-1, μm.

The expression "in the absence of suspending agents" means the absenceof substances which, depending on the type and the amount, would becapable of suspending the graft monomers IV in the aqueous phase. Thedefinition does not exclude the presence of substances which, forexample, have acted as suspending agents in the preparation of a graftedgrafting base III; in such cases, the coagulating agent or precipitatingagent which is used to break the latex III has to be added in an amountwhich compensates the suspending action of the substances employed inthe previous stage; in other words, care must be taken to ensure thatthe graft monomers IV do not form a (stable) emulsion or dispersion inthe aqueous phase.

A graft polymer for component (d), prepared in this way in the absenceof suspending agents, can be dispersed, as a component of the mouldingcompositions according to the invention, in the other resin componentsto give an extremely small particle size, which remains relativelyunchanged even over fairly long processing periods at elevatedtemperature.

The expression "extremely small particle size" means that the number,shape and size of the graft polymer particles to be employed essentiallycorrespond, even after the homogenisation procedure, to the number,shape and size of the graft polymer particles introduced into themolten, other resin components.

It is also possible to use, as the grafting base III, those acrylaterubbers which are obtained as an aqueous emulsion (latex), and the latexparticles of which contain 1-20% by weight, preferably 1-10% by weight,relative to III, of monomers which are already grafted on in aqueousemulsion and whose homopolymers or copolymers would have glasstransition temperatures >0° C.

Preferred grafted-on monomers of this type are alkyl acrylates, alkylmethacrylates, styrene, acrylonitrile,α-methylstyrene and/or vinylacetate.

Grafting bases III of this type are prepared by, for example, emulsionpolymerisation or emulsion graft polymerisaion. However, they can alsobe prepared by preparing an acrylate rubber by solution or masspolymerisation, then grafting on the graft monomers, and thereafterconverting these rubbers to an aqueous emulsion which is suitable forfurther grafting processes.

Suitable grafting bases III for acrylate rubbers of this particularembodiment are therefore, in addition to the polymers listed on page 19,graft polymers which have been prepared in aqueous emulsion fromacrylate polymers or copolymers which, if appropriate, contain a dienerubber core, and ethylenically unsaturated polymerisable monomers.

In the context of the invention, polyalkylene terephthalates forcomponent (e) are reaction products of aromatic dicarboxylic acids ortheir reactive derivatives (for examole dimethyl esters or anhydrides)and aliphatic, cycloaliphatic or araliphatic diols, and mixtures ofthese reaction products.

Preferred polyalkylene terephthalates for component (e) can be preparedfrom terephthalic acid (or its reactive derivatives) and aliphatic orcycloaliphatic diols having 2-10 C atoms, by known methods (KunststoffHandbuch (Plastics Handbook), Vol. VIII, page 695 et seq, Carl HanserVerlag, Munich 1973).

Preferred polyalkylene terephthalates for component (e) contain at least80, preferably at least 90, mol % relative to the dicarboxylic acidcomponent, of terephthalic acid radicals, and at least 80, preferably atleast 90, mol %, relative to the diol component, of ethylene glycoland/or 1,4-butanediol radicals.

The preferred polyalkylene terephthalates (e) can contain, in additionto terephthalates, up to 20 mol % of radicals of other aromaticdicarboxylic acids having 8-14 C atoms or aliphatic dicarboxylic acidshaving 4-12 C atoms, such as, for example, radicals of phthalic acid,isophthalic acid, naphthalene-2,6-dicarboxylic acid,4,4'diphenyldicarboxylic acid, succinic acid, adipic acid, sebacic acid,azelaic acid or cyclohexanediacetic acid.

The preferred polyalkylene terephthalates (e) can contain, in additionto ethylene glycol or 1,4-butanediol radicals, up to 20 mol % of otheraliphatic diols having 3-12 C atoms or cycloaliphatic diols having 6-21C atoms, for example radicals of 1,3-propanediol,2-ethyl-1,3-propanediol, neopentylglycol, 1,5-oentanediol, 1,6-hexanediol, cyclohexane-1,4-dimethanol, 3-methyl-2,4-pentanediol,2-methyl-2,4-pentanediol, 2,2,4-trimethyl-1,3-pentanediol,2,2,4-trimethyl-1,6-pentanediol, 2-ethyl1,3-hexanediol,2,2-diethyl-1,3-propanediol, 2,5-hexanediol,1,4-di-(β-hydroxyethoxy)-benzene, 2,2-bis-(4-hydroxycyclohexyl)-propane,2,4-dihydroxy-1,1,3,3-tetramethylcyclobutane,2,2-bis-(3-β-hydroxyethoxyphenyl)-propane and2,2-bis-(4-hydroxypropoxyphenyl)-propane (German OffenlegungsschriftenNos. 2,407,647, 2,407,776 and 2,715,932).

The polyalkylene terephthalates for component (e) can be branched byincorporating relatively small amounts of trihydric or tetrahydricalcohols or tribasic or tetrabasic carboxylic acids, as described in,for example, German Offenlegungsschrift No. 1,900,270 and U.S. Pat. No.3,692,744. Examples of preferred branching agents are trimesic acid,trimellitic acid, trimethylolethane and -propane and pentaerythritol. Itis advisable to use no more than 1 mol % of the branching agent,relative to the acid component.

Particularly preferred polyalkylene terephthalates (e) are those whichhave been prepared solely from terephthalic acid and its reactivederivatives (for example its dialkyl esters) and ethylene glycol and/or1,4-butanediol, and mixtures of these polyalkylene terephthalates.

Other preferred polyalkylene terephthalates (e) are copolyesters whichare prepared from at least two of the abovementioned alcohol components;particularly preferred copolyesters are poly-(ethyleneglycol/1,4-butanediol) terephthalates.

The polyalkylene terephthalates preferably used as component (e)generally have an intrinsic viscosity of 0.4-1.5 dl/g, oreferably0.5-1.3 dl/g, in particular 0.6-1.2-dl/g, measured inphenol/o-dichlorobenzene (1:1 parts by weight) at 25° C. in each case.

To further increase the petrol-resistance of the mixtures according tothe invention which contain the components (a), (d) and, if appropriate,(e), up to 5% by weight, relative to the total weight of the components(a) (d) and, if appropriate, (e), of ethylene homopolymers or copolymerscan also be added. In this context, ethylene copolymers arepolyethylenes the radicals of which, in addition to consisting ofethylene radicals, consist of up to 30% by weight, relative to theethylene copolymer, of radicals of other copolymerisable monomers, suchas, for example, (meth)acrylic acid.

The moulding compositions according to the invention which are based onthe components (a), (d) and, if appropriate, (e), can contain theadditives customarily used in polycarbonate chemistry, rubber chemistryand polyester chemistry, such as lubricants, mould-release agents,nucleating agents, stabilisers, fillers, reinforcing substances,flameproofing agents and dyestuffs.

The moulding compositions containing fillers and reinforcing agents andbased on the components (a), (d) and, if appropriate, (e), can containup to 30% by weight, relative to the reinforced moulding composition, offillers and/or reinforcing substances. Preferred reinforcing substancesare glass fibres. Preferred fillers which can also have a reinforcingeffect are glass spheres, mica, silicates, quartz, talc, titaniumdioxide and wollastonite.

The moulding compositions which contain flameproofing agents and arebased on the components (a)+(d) and, if appropriate, (e), can containflameproofing agents in a concentration of, in general, less than 30% byweight, relative to the flameproofed moulding compositions. Allflameproofing agents known to be used for polyester mouldingcompositions are suitable, such as, for example, polyhalogenodiohenyl,polyhalogenodiphenyl ethers, polyhalogenophthalic acid and itsderivatives and polyhalogenooligo-and -polycarbonates, the correspondingbromine comoounds being particularly effective. Synergistic agents, suchas, for example, antimony trioxide, can also be used concomitantly.

The moulding compositions according to the invention which are based onthe components (a), (d) and, if appropriate, (e) can be prepared in thecustomary mixing units, such as mills, kneaders and single-screw andmultiple-screw extruders. The moulding compositions according to theinvention which are based on the components (a), (d) and, ifappropriate, (e) can be processed to shaped articles which exhibit anextremely small amount of distortion, even when subjected to a thermalload for a relatively long time. Although, in most cases, the resincomponents (a), (d) and (e) are advantageously mixed in a single step,it may sometimes also be advisable initially to omit one component, andonly to admix this subsequently.

The following polymers were used in the examples listed:

(d1) A polymer which consists of 75% by weight of a grafting basecomposed of crosslinked polybutadiene (gel content above 70%, measuredin toluene) and 25% by weight of a graft composed of 28% ofacrylonitrile and 72% of styrene, the particle diameter of the graftingbase in latex form being between 0.3 and 0.4 μm.

(d2) A polymer which consists of a grafting base composed of 79.2 partsby weight of n-butyl acrylate, which is crosslinked with 0.4 part byweight of butylene 1,3-diacrylate and in which 0.4 part by weight ofdiallyl maleate is incorporated in the form of graft monomers, and of agraft composed of 20 parts by weight of a polymethacrylate.

The following polydiorganosiloxane/polycarbonate block copolymers wereused in the examples listed:

(a1) A copolycarbonate which is based on bisphenol A and 4.5% by weightof polydimethylsiloxane having a block length (P_(n)) of 40, and has arelative solution viscosity of 1.31 (measured in CH₂ Cl₂ at 25° C. andat a concentration of 0.5 g/100 ml).

The determination of the siloxane content, that is to say the proportionof dimethylsiloxy units in % by weight, relative to the total weight ofthe block copolymer, is carried out gravimetrically and by nuclearresonance spectrometry. The mean siloxane block length is stated as thedegree of polymerisation P_(n) found by determining the terminal groupsin the siloxane prepolymer.

(a3) For the comparative examples, a homopolycarbonate based onbisphenol A and having a relative solution viscosity of 1.29 was used.

(e) A polybutylene terephthalate having an intrinsic viscosity of 1.18dl/g, measured in phenol/o-dichlorobenzene (1:1) at 25° C., was alsoused in the examples listed.

In some cases, an ethylene copolymer containing 4% by weight of acrylicacid and 12% by weight of tert.butyl acrylate, as well as a heatstabiliser and pigments in the form of a concentrate in bisphenolA/polycarbonate were also used.

The preparation of the moulding compositions based on the components(a), (d) and, if appropriate, (e) was carried out by melting andhomogenising in a suitable unit. Processing was carried out on aninjection moulding machine.

The determination of the mechanical strength in the tensile test wascarried out on 70% proportional bars, on the basis of DIN 53,455/ISO R527.

The notched impact strength was determined on flat bars (80 mm×10 mm×4mm) having a V-shaped notch 2.7 mm deep, on the basis of DIN 53, 452/ISOR 179.

The critical width was determined in accordance with ASTM D 256.

The impact penetrationttest in accordance with DIN 53,443 ischaracterised by an assessment of the fracture behaviour (3=tough -brittle, 4=tough).

The determination of the heat-distortion resistance by the Vicat (B)method was carried out in accordance with DIN 53,460/ISO 360. Theresistance to petrol was tested in a screen test, during an immersiontime of 5 minutes and with 0.6% outer fibre elongation, againstsimulated premium-grade petrol in the form of 1:1 isooctane/toluene andisooctane (42.5%)/toluene (42.5%) methanol (15%) (M-15).

                                      TABLE 1                                     __________________________________________________________________________                             Example 1                                                                            Example 2                                     Composition          Unit                                                                              (Comparison)                                                                         (Comparison)                                                                         Example 3                                                                            Example 4                       __________________________________________________________________________    Homopolycarbonate (a3)                                                                             %   95     95     --     --                              Copolycarbonate (a1) %   --     --     95     95                              Polymer (d1)         %    5     --      5     --                              Polymer (d2)         %   --      5     --      5                              Ethylene copolymer   %   --     --     --     --                              Polybutylene terephthalate (e)                                                                     %   --     --     --     --                              Yield stress         MPa 60     60     55     55                              Tensile strength     MPa 68     75     54     52                              Elongation at break  %   120    125    80     87                              Notched impact strength                                                       at room temperature  kJ/m.sup.2                                                                        47     47     37     41                              at-40° C.     kJ/m.sup.2                                                                        12      9     27     29                              Critical width                                                                at room temperature  mm  >8     7.6-7.8                                                                              >8     >8                              at 0° C.      mm  6.5-6.8                                                                              --     >8     >8                              at -20° C.    mm  --     --     >8     >8                              Impact penetration test at -40° C.:                                                             10 × 4                                                                         10 ×  4                                                                        2 × 4/8 × 3                                                              3 × 4/7 × 3         fracture behaviour                                                            Damaging energy      J   75     70     54     50                              Vicat B temperature  °C.                                                                        145    145    146    145                             Petrol resistance                                                             against 1:1 isooctane/toluene                                                                          fracture                                                                             fracture                                                                             cracks cracks                          against M-15 (isooctane/toluene/methanol)                                                              cracks cracks fracture                                                                             a few cracks                    __________________________________________________________________________                             Example 5                                                                            Example 6                                     Composition          Unit                                                                              (Comparison)                                                                         (Comparison)                                                                         Example 7                                                                            Example 8                       __________________________________________________________________________    Homopolycarbonate (a3)                                                                             %   44     44     --     --                              Copolycarbonate (a1) %   --     --     44     44                              Polymer (d1)         %    5     --      5     --                              Polymer (d2)         %   --      5     --      5                              Ethylene copolymer   %    2      2      2      2                              Polybutylene terephthalate (e)                                                                     %   40     40     40     40                              Colorant concentrate.sup.(1)                                                                       %    7      7      7      7                              Heat stabiliser.sup.(2)                                                                            %    2      2      2      2                              Yield stress         MPa 55     58     51     54                              Tensile strength     MPa 59     59     55     56                              Elongation at break  %   136    133`   126    128                             Notched impact strength                                                       at room temperature  kJ/m.sup.2                                                                        43     19     43     41                              at -40°  C.   kJ/m.sup.2                                                                        14      9     15     13                              Critical width                                                                at room temperature  mm  5.8-6.0                                                                              <4     >8     >8                              at 0° C.      mm  --     --     7.0-7.2                                                                              4.9-5.1                         at -20° C.    mm  --     --     --     --                              Impact penetration test at -40° C.:                                                             7 × 4/3 × 3                                                              2 × 4/8 × 3                                                              10 × 4                                                                         9 × 4/1 × 3         fracture behaviour                                                            Damaging energy      J   65     69     62     69                              Vicat B temperature  °C.                                                                        122    123    122    124                             Petrol-resistance                                                             against 1:1 isooctane/toluene                                                                          cracks cracks a few cracks                                                                         a few cracks                    against M-15 (isooctane/toluene/methanol)                                                              no cracks                                                                            no cracks                                                                            no cracks                                                                            no cracks                       __________________________________________________________________________                             Example 9                                            Composition          Unit                                                                              (Comparison)                                                                         Example 10                                                                           Example 11                                                                           Example 12                      __________________________________________________________________________    Homopolycarbonate (a3)                                                                             %   --     --     --     --                              Copolycarbonate (a1) %   49     39     34     54                              Polymer (d1)         %   --     10     --     --                              Polymer (d2)         %   --     --      5      5                              Ethylene copolymer   %    2      2      2      2                              Polybutylene terephthalate (e)                                                                     %   40     40     50     30                              Colorant concentrate.sup.(1)                                                                       %    7      7      7      7                              Heat stabiliser.sup.(2)                                                                            %    2      2      2      2                              Yield stress         MPa 59     44     53     54                              Tensile strength     MPa 56     51     51     57                              Elongation at break  %   112    150    149    108                             Notched impact strength                                                       at room temperature  kJ/m.sup.2                                                                        26     41     34     44                              at -40° C.    kJ/m.sup.2                                                                        13     17     10     15                              Critical width                                                                at room temperature  mm  5.6-5.8                                                                              >8     >8     >8                              at 0° C.      mm  --     >8     <4     6.5-6.7                         at -20° C.    mm  --     5.1-5.4                                                                              --     --                              Impact penetration test at -40° C.:                                                             10 × 4                                                                         10 × 4                                                                         7 × 4/3 × 3                                                              10 × 4                    fracture behaviour                                                            Damaging energy      J   70     59     54     62                              Vicat B temperature  °C.                                                                        125    115    123    123                             Petrol-resistance                                                             against 1:1 isooctane/toluene                                                                          cracks no cracks                                                                            a few cracks                                                                         cracks                          against M-15 (isooctane/toluene/methanol)                                                              no cracks                                                                            no cracks                                                                            no cracks                                                                            no cracks                       __________________________________________________________________________     .sup.(1) Grey pigment; effective amount 1% by weight;                         .sup.(2) Tris(3ethyl-oxethanyl-3-methyl)phosphite, effective amount 0.1%      by weight                                                                

We claim:
 1. A thermoplastic moulding composition containing (a) apolydiorganosiloxane polycarbonate block copolymer having an averagemolecular weight M_(w) of 10,000 to 200,000 and containing between 75%by weight and 97.5% by weight of aromatic carbonate structural units andbetween 25% by weight and 2.5% by weight of polydiorganosiloxanestructural units, the block copolymers being prepared frompolydiorganosiloxanes which contain α,Ψ-bis-hydroxyaryloxy terminalgroups and have a degree of polymerisation P_(n) of 5 to 100,(d) 5-20parts by weight of an elastomeric polymer having a glass transitiontemperature of below -20° C. which is(i) graft copolymers comprisingbutadiene/styrene copolymers, poly(meth)acrylates or polybutadienes ontowhich are grafted styrene, acrylonitriel, (meth)acrylates, or mixturesthereof, (ii) ethylene vinylacetate copolymers containing 15-70% byweight vinylacetate and having melt indices from non-freeflowing to1000, or (iii) epm or epdm rubbers in which the weight ratio of ethyleneradicals to propylene radicals is in the range from 40:60 to 90:10; and(e) 0-50 parts by weight of thermoplastic polyalkylene terephthalate,the sum of the number of parts by weight of components (a)+(d)+(e) being100 parts by weight in each case.
 2. A composition as claimed in claim 1comprising 30 to 90 parts by weight of component (a) and 5 to 20 partsby weight of component (d).
 3. A composition as claimed in claim 1wherein the component (d) has a gel content of move than 20% by weight.4. A composition as claimed in claim 1 wherein the component (d) is anethylenevinyl acetate copolymer containing 15-70% by weight of vinylacetate and having a melt index from non-freeflowing to 1,000.
 5. Acomposition as claimed in any of claim 1 wherein the component (d) is anEPM or EPDM rubber in which the weight ratio of ethylene radicals topropylene radicals is in the range from 40:60 to 90:10.
 6. A compositionas claimed in claim 1 wherein the component (d) is a graft polymerobtainable by graftingI. 10-40% by weight, relative to the graftedproduct, of at least one (meth)acrylate and/or a mixture of 10-35% byweight, relative to the mixture, of acrylonitrile and 65-90% by weight,relative to the mixture, of styrene onto II. 60-90% by weight, relativeto the grafted product, of a butadiene polymer containing at least 70%by weight, relative to II, of butadiene radicals as the grafting base.7. A composition as claimed in claim 1 wherein the component (d) is agraft polymer with a glass transition temperature below -20° C. andcomprisesIII. as the grafting base, 25-95% by weight, relative tocomponent (d), of an acrylate rubber having a glass transitiontemperature of below -20° C., and IV. as the grafting monomer, 2-75% byweight, relative to component (d), of at least one polymerisableethylenically-unsaturated monomer whose homopolymer or copolymer formedin the presence of III have a glass transition temperature of above 25°C.
 8. A composition as claimed in claim 7 wherein the grafting monomerIV is α-methylstyrene, styrene, acrylonitrile,, methyl methacrylate or amixture thereof.
 9. A composition aS claimed in claim 7 wherein thecomponent (d) is prepared by grafting 2-20% by weight, relative to (d)of monomer IV onto 80-98% by weight, relative to (d), of the latex ofIII, which has been completely broken and suspended in water, in theabsence of suspending agents.
 10. A composition as claimed in any ofclaim 1 wherein component (e) contains at least 80 mol %, relative tothe dicarboxylic acid component, of terephthalic acid radicals, and atleast 80 mol %, relative to the diol component, of ethylene glycoland/or 1,4-butanediol radicals.
 11. A composition as claimed in claim 1wherein component (e) contains, in addition to terephthalates, up to 20mol % of radicals of other aromatic dicarboxylic acids having 8-14 Catoms or aliphatic dicarboxylic acids having 4-12 C atoms.
 12. Acomposition as claimed in any of claim 1 which additionally contains anethylene homopolymer or copolymer the radicals of which consist of up to30% by weight, relative to the ethylene copolymer in each case, ofradicals of other copolymerisable monomers.
 13. A composition as claimedin claim 12 wherein the ethylene homopolymer or copolymer is present inan amount up to 5% by weight, relative to the total weight of (a), (d)and (e).
 14. A composition as claimed in claim 12, also includinglubricant, mould-release agent, nucleating agent, stabiliser, filler,reinforcing substance, dyestuff and/or flameproofing agent.
 15. Mouldedproducts made from a composition as claimed in claim 1.